723361006: familiair multipel fibrofolliculoom (aandoening)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2020. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

3424234017 Familial multiple fibrofolliculoma (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

3424235016 Familial multiple fibrofolliculoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

6586861000146112 familiair multipel fibrofolliculoom nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

6586871000146118 familiair multipel fibrofolliculoom (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

3424236015 A genodermatosis with characteristics of the presence of multiple hamartomas of the hair follicle. It has been described in one family so far. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
familiair multipel fibrofolliculoom	Is a	Autosomal dominant hereditary disorder	false	Inferred relationship	Some
familiair multipel fibrofolliculoom	Is a	Familial neoplastic disease	false	Inferred relationship	Some
familiair multipel fibrofolliculoom	Is a	Genodermatosis	false	Inferred relationship	Some
familiair multipel fibrofolliculoom	Is a	Fibrofolliculoma	false	Inferred relationship	Some
familiair multipel fibrofolliculoom	Is a	Hereditary disorder of the integument	false	Inferred relationship	Some
familiair multipel fibrofolliculoom	Occurrence	Congenital	false	Inferred relationship	Some	2
familiair multipel fibrofolliculoom	Occurrence	Congenital	false	Inferred relationship	Some	3
familiair multipel fibrofolliculoom	Associated morphology	Follicular fibroma	false	Inferred relationship	Some	2
familiair multipel fibrofolliculoom	Finding site	Hair follicle structure	false	Inferred relationship	Some	2
familiair multipel fibrofolliculoom	Associated morphology	gebrekkige ontwikkeling (afwijkende morfologie)	false	Inferred relationship	Some	3
familiair multipel fibrofolliculoom	Finding site	Skin structure	false	Inferred relationship	Some	3
familiair multipel fibrofolliculoom	Associated morphology	Follicular fibroma	false	Inferred relationship	Some	1
familiair multipel fibrofolliculoom	Finding site	Hair follicle structure	false	Inferred relationship	Some	1
familiair multipel fibrofolliculoom	Occurrence	Congenital	false	Inferred relationship	Some	1
familiair multipel fibrofolliculoom	Pathological process (attribute)	Pathological developmental process	false	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Concept inactivation indicator reference set

REPLACED BY association reference set (foundation metadata concept)